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Parallel import of medicinal products: regulatory update

European Pharmaceutical Review

This concerns the quantity of the medicinal product in the packaging, ie, the increase or decrease in the number of units of the product in the outer packaging according to local demands and its labelling, including the leaflet, which should be in the language of the country into which the product is imported.

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Complex generics: Are global regulators addressing the needs?

Quality Matters

Complex generics: Are global regulators addressing the needs? The development of generic versions of innovator medicines is a global public health need. Quality standards in particular help ensure medicines are safe, work as intended, and are available when needed, no matter the company producing them or where they are made.

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Essential elements of a strong, global medicines supply chain

Quality Matters

host year for APEC in 2023. In my keynote remarks, I highlighted the following elements of a strong medicines supply chain. Adherence to standards facilitates a supply of medicines with consistent quality, no matter which company produces them or where they are made. josh.levin@usp.org Wed, 04/26/2023 - 16:11 Supply Chain

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Standards support medicines supply chain resilience and the future of quality

Quality Matters

Quality across the product lifecycle The role of standards goes far beyond the drug manufacturing process – from the sourcing of raw materials to packaging, labeling, distribution, and point-of-care administration – to help ensure quality across the pharmaceutical product lifecycle. kristine.gates… Thu, 04/20/2023 - 08:51 Supply Chain